The Specialist I, Country Study Enablement assists in the coordination and administration of local study activities throughout the entire study cycle to ensure quality and consistency of study deliverables to time, cost and quality objectives.

Typical Accountabilities

Responsible for local study payment related issues, include but not limited to: site payment, EC payment, translation payment, printing payment, drug payment, depot payment and CRO, SMO, PRO payment.Organize external meetings by following procurement guidance, such as investigator meeting, city meeting, monitoring meeting, inspection meeting.Administration support to newcomer on board or leaving tasks, and logistics support for internal team meeting.Responsible for clinical trial related device purchasing and management.Coordinate with procurement and CSM to organize vendor bidding and PR set up for CRO, SMO and PRO.Responsible for Trial Disclosure in CDE website before FSI and follow up ongoing updates.Support SEPI/CSM to confirm site contract template and study country CSA master version format checking.Additional country-specific tasks depending on country study needs.

Education, Qualifications, Skills and Experience

Essential

Bachelor degree or above in healthcare-related field, or equivalent.At least 1-year experience as CTA/CTC/CRC or equivalent experience.Knowledge in clinical study process and understanding of the ICH/GCP guideline.Good interpersonal skills and ability to work in an international team environment.Ability to train others on study administration procedures.Good computer skills in Microsoft and other software.Proficient written and verbal communication skills, collaboration and interpersonal skills.Proven organizational and administrative skills.Fluent in both oral and written English.

Desirable

Ability to develop advanced computer skills to increase efficiency in day-to-day tasks.Display excellent organization and time management skills, excellent attention to detail, and ability to multi-task in a high-volume environment with shifting priorities.Team oriented and flexible; ability to respond quickly to shifting demands and opportunities.Demonstrates ability to prepare and deliver study related training materials.

【AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.
阿斯利康是一家提供平等机会的企业，我们将考虑所有符合条件的求职者就业。不因残疾、性别或性取向、怀孕或产假状况、种族或民族或族裔出身、年龄、宗教或信仰、性别认同或变更、婚姻或伴侣关系、受保护的退伍军人身份（如果适用）及任何其他受法律保护的特征而产生歧视。】

Date Posted

06-1月-2025

Closing Date

13-1月-2025

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.